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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1023504Generated: October 26, 2026

p-Fluoronitrobenzene → 1-Ethoxy-3-(4-nitrophenoxy)benzene

https://huagongshe.com/reaction/1023504

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-FluoronitrobenzeneHCID 9590—
ReactantPotassium CarbonateHCID 11430—
Reactant3-EthoxyphenolHCID 69306—
SolventDimethylformamideHCID 6228—
Product1-Ethoxy-3-(4-nitrophenoxy)benzeneHCID 67234996170.6%

Reaction Conditions

Temperature120 °C

Reaction Steps

The two reactions were performed in parallel. Two microwave vials were set up in parallel. In a large 30 mL microwave vial, 3-(ethyloxy)phenol (2 times 1.25 g, 9.045 mmol) was dissolved in 6 mL of dimethylformamide. 1-Fluoro-4-nitrobenzene (2 times 1.28 g, 9.045 mmol) and potassium carbonate (2 times 3.75 g, 27.15 mmol) were added. The reaction mixture was heated under microwave irradiation during 1 hour at 120° C. The combined reaction mixtures were filtered. The filtrated solid was washed with dichloromethane. The volatiles were evaporated under vacuum. Some dichloromethane and brine were added to this crude. The compound was extracted with dichloromethane (2 times) and ethyl acetate (2 times). The combined organic phases were dried over sodium sulphate. This afforded the title compound (4 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08722695B2
Source datasetuspto-grants-2014_05
ORD IDord-740ee47c7c224185a26e3c36a5cb93bd
Source noteuspto-grants-2014_05